Early detection is the key to curing prostate cancer. The American Urologic Association (AUA) recommends that men over 40 undergo a Prostate Specific Antigen (PSA) blood test and digital rectal exam (DRE). Prostate cancer before age 50 is uncommon. However, African-American men and men with a family history of the disease are at a higher risk for developing prostate cancer at a younger age. Your physician can determine the best regimen for you.
A PSA blood test and digital rectal exam (DRE) are the two standard screening tests for prostate cancer. PSA is an enzyme produced by the prostate. PSA is produced by both normal and prostate cancer cells. Small amounts of this enzyme in the bloodstream are normal and an elevated PSA alone does not necessarily indicate cancer. Normal levels are less than 4.0 ng/ml. Levels higher than this should be evaluated. Benign elevations of PSA can be caused by an enlarged prostate, prostate inflammation, infection or trauma. Often, the DRE does not reveal any abnormality. Occasionally, the PSA will be low, but the DRE will be abnormal. For this reason, the PSA blood test together with the DRE is important for early detection. Prostate cancer cells make PSA even if they are outside the gland.
The PSA is also used for monitoring results after treatment. If prostate cancer cells have spread to the bone or lymph nodes, these cells will make PSA. After surgery, the PSA is likely to drop quickly. After any form of radiation (IMRT, Seeds, etc.) the PSA drops more slowly as the cells die off over time. Thus, it may take several years to reach the lowest post-treatment PSA level (nadir) after any form of radiation treatment.
A transrectal biopsy using an ultrasound guided approach is the standard approach for biopsying the prostate. This is usually performed by a urologist. The standard is 12-16 cores. The pathologist will grade the cancer using the Gleason Scoring system and likely will state how much of the core is involved with cancer. The number of positive biopsy cores involved can influence the treatment recommendations.
Staging prostate cancer is based on the physical exam and any diagnostic studies performed (CT, MRI and/or Bone scans). Some patients do not require diagnostic scans. If there is no palpable nodule in the gland, the Stage is T1. T1 means there is no palpable disease and is divided into 3 categories based on how it was diagnosed. T1a and T1b are reserved for patients in which the cancer was found while removing part of the gland to relieve blockage, this procedure is called a TURP (transurethral resection of the prostate). T1c is usually detected by an elevated PSA. Note that even if the pathology shows disease on both sides of the gland, this does not affect the clinical stage.
T2a refers to a small nodule on one side of the gland, T2b means that the nodule occupies most of one lobe, and T2c means that the nodule occupies parts of both lobes. T3 is quite rare and means that the nodule extends outside the gland.
Every patient at Lakewood Ranch Oncology Center is evaluated for Stage, Grade and PSA. Studies have demonstrated that patients can be grouped into risk groups that behave in similar ways. These risk groups can be useful for evaluating results of various treatments and to make treatment decisions. The risk groupings currently being adopted by most major centers are Low, Intermediate and High Risk. It is valuable for you to determine in which group you fall so that you can discuss it with your physician.
Low Risk: Stage T1 to T2a•PSA less than or
equal to 10 ng/ml•Gleason Score 6 or less
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Intermediate Risk: PSA 10.1-20
or Gleason score 7•or Stage T2b only
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High Risk: PSA > 20•or T2c/T3
or Gleason Score 8-10•or 2 of the intermediate risk factors